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Citation Kirienko NV, McEnerney JD, Fay DS. Coordinated regulation of intestinal functions in C. elegans by LIN-35/Rb and SLR-2. PLoS Genet, 2008.
PubMed ID 18437219
Short Description Coordinated regulation of intestinal functions in C. elegans by LIN-35/Rb and SLR-2.
GEO Record: GSE9246 Platform: GPL200
Download gene-centric, log2 transformed data: WBPaper00031832.ce.mr.csv
# of Conditions 6
Full Description 1316625150_help LIN-35 is the sole C. elegans representative of the pocket protein family, which includes the mammalian Retinoblastoma protein pRb and its paralogs p107 and p130. In addition to having a well-established and central role in cell cycle regulation, pocket proteins have been increasingly implicated in the control of critical and diverse developmental and cellular processes. To gain a greater understanding of the roles of pocket proteins during development, we have characterized a synthetic genetic interaction between lin-35 and slr-2, which we show encodes a C2H2-type Zn-finger protein. Whereas animals harboring single mutations in lin-35 or slr-2 are viable and fertile, lin-35; slr-2 double mutants arrest uniformly in early larval development without obvious morphological defects. Using a combination of approaches including transcriptome profiling, mosaic analysis, starvation assays, and expression analysis, we demonstrate that both LIN-35 and SLR-2 act in the intestine to regulate the expression of many genes required for normal nutrient utilization. These findings represent a novel role for pRb family members in the maintenance of organ function. Our studies also shed light on the mechanistic basis of genetic redundancy among transcriptional regulators and suggest that synthetic interactions may result from the synergistic misregulation of one or more common targets.
Experimental Details:
WBPaper00031832:N2_1
WBPaper00031832:N2_2
WBPaper00031832:N2_3
WBPaper00031832:slr-2_1
WBPaper00031832:slr-2_2
WBPaper00031832:slr-2_3.
Tags 1316625150_help
Method: microarray, Species: Caenorhabditis elegans, Topic: WT vs. mutant